ES2655871T3 - Método para producir olefinas fluoradas - Google Patents
Método para producir olefinas fluoradas Download PDFInfo
- Publication number
- ES2655871T3 ES2655871T3 ES08798495.1T ES08798495T ES2655871T3 ES 2655871 T3 ES2655871 T3 ES 2655871T3 ES 08798495 T ES08798495 T ES 08798495T ES 2655871 T3 ES2655871 T3 ES 2655871T3
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- ES
- Spain
- Prior art keywords
- formula
- compound
- catalyst
- reaction
- phase
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 238000000034 method Methods 0.000 title claims abstract description 48
- 150000001336 alkenes Chemical class 0.000 title description 6
- 238000006243 chemical reaction Methods 0.000 claims abstract description 79
- 150000001875 compounds Chemical class 0.000 claims abstract description 54
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 16
- 229910052731 fluorine Inorganic materials 0.000 claims abstract description 12
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 7
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 claims abstract description 6
- 229910000040 hydrogen fluoride Inorganic materials 0.000 claims abstract description 6
- 229910052740 iodine Inorganic materials 0.000 claims abstract description 6
- 150000002894 organic compounds Chemical class 0.000 claims abstract 2
- 239000003054 catalyst Substances 0.000 claims description 65
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 30
- 239000000460 chlorine Substances 0.000 claims description 16
- VMPVEPPRYRXYNP-UHFFFAOYSA-I antimony(5+);pentachloride Chemical compound Cl[Sb](Cl)(Cl)(Cl)Cl VMPVEPPRYRXYNP-UHFFFAOYSA-I 0.000 claims description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 8
- 238000010574 gas phase reaction Methods 0.000 claims description 6
- 229910052787 antimony Inorganic materials 0.000 claims description 4
- -1 antimony halide Chemical class 0.000 claims description 4
- FDMFUZHCIRHGRG-UHFFFAOYSA-N 3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C=C FDMFUZHCIRHGRG-UHFFFAOYSA-N 0.000 claims description 3
- FAPDDOBMIUGHIN-UHFFFAOYSA-K antimony trichloride Chemical compound Cl[Sb](Cl)Cl FAPDDOBMIUGHIN-UHFFFAOYSA-K 0.000 claims description 3
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 3
- FFTOUVYEKNGDCM-OWOJBTEDSA-N (e)-1,3,3-trifluoroprop-1-ene Chemical compound F\C=C\C(F)F FFTOUVYEKNGDCM-OWOJBTEDSA-N 0.000 claims 2
- 239000012071 phase Substances 0.000 description 20
- FXRLMCRCYDHQFW-UHFFFAOYSA-N 2,3,3,3-tetrafluoropropene Chemical compound FC(=C)C(F)(F)F FXRLMCRCYDHQFW-UHFFFAOYSA-N 0.000 description 15
- 239000007795 chemical reaction product Substances 0.000 description 15
- 239000007789 gas Substances 0.000 description 12
- 238000006704 dehydrohalogenation reaction Methods 0.000 description 9
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 8
- 239000011737 fluorine Substances 0.000 description 8
- GCLGEJMYGQKIIW-UHFFFAOYSA-H sodium hexametaphosphate Chemical compound [Na]OP1(=O)OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])OP(=O)(O[Na])O1 GCLGEJMYGQKIIW-UHFFFAOYSA-H 0.000 description 7
- 239000007791 liquid phase Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 5
- 238000000926 separation method Methods 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- FDOPVENYMZRARC-UHFFFAOYSA-N 1,1,1,2,2-pentafluoropropane Chemical compound CC(F)(F)C(F)(F)F FDOPVENYMZRARC-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- 239000006227 byproduct Substances 0.000 description 4
- 229910052736 halogen Inorganic materials 0.000 description 4
- 150000002367 halogens Chemical class 0.000 description 4
- OQISUJXQFPPARX-UHFFFAOYSA-N 2-chloro-3,3,3-trifluoroprop-1-ene Chemical compound FC(F)(F)C(Cl)=C OQISUJXQFPPARX-UHFFFAOYSA-N 0.000 description 3
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 238000003682 fluorination reaction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- SMCNZLDHTZESTK-UHFFFAOYSA-N 2-chloro-1,1,1,2-tetrafluoropropane Chemical compound CC(F)(Cl)C(F)(F)F SMCNZLDHTZESTK-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- 229910000792 Monel Inorganic materials 0.000 description 2
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 239000006229 carbon black Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- 238000005796 dehydrofluorination reaction Methods 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 238000003541 multi-stage reaction Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000000746 purification Methods 0.000 description 2
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
- 150000003624 transition metals Chemical class 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- SHXHPUAKLCCLDV-UHFFFAOYSA-N 1,1,1-trifluoropentane-2,4-dione Chemical compound CC(=O)CC(=O)C(F)(F)F SHXHPUAKLCCLDV-UHFFFAOYSA-N 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 description 1
- 229910010165 TiCu Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000003082 abrasive agent Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000007259 addition reaction Methods 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000003989 dielectric material Substances 0.000 description 1
- 229910001873 dinitrogen Inorganic materials 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000005485 electric heating Methods 0.000 description 1
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000004334 fluoridation Methods 0.000 description 1
- 239000012025 fluorinating agent Substances 0.000 description 1
- 239000004446 fluoropolymer coating Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 229910000856 hastalloy Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 238000005647 hydrohalogenation reaction Methods 0.000 description 1
- 229910001026 inconel Inorganic materials 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 229940074869 marquis Drugs 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- VBUNOIXRZNJNAD-UHFFFAOYSA-N ponazuril Chemical compound CC1=CC(N2C(N(C)C(=O)NC2=O)=O)=CC=C1OC1=CC=C(S(=O)(=O)C(F)(F)F)C=C1 VBUNOIXRZNJNAD-UHFFFAOYSA-N 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- 239000012629 purifying agent Substances 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000003507 refrigerant Substances 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052707 ruthenium Inorganic materials 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- QHMQWEPBXSHHLH-UHFFFAOYSA-N sulfur tetrafluoride Chemical compound FS(F)(F)F QHMQWEPBXSHHLH-UHFFFAOYSA-N 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/013—Preparation of halogenated hydrocarbons by addition of halogens
- C07C17/04—Preparation of halogenated hydrocarbons by addition of halogens to unsaturated halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/07—Preparation of halogenated hydrocarbons by addition of hydrogen halides
- C07C17/087—Preparation of halogenated hydrocarbons by addition of hydrogen halides to unsaturated halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/202—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction
- C07C17/206—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms two or more compounds being involved in the reaction the other compound being HX
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/20—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms
- C07C17/21—Preparation of halogenated hydrocarbons by replacement by halogens of halogen atoms by other halogen atoms with simultaneous increase of the number of halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/25—Preparation of halogenated hydrocarbons by splitting-off hydrogen halides from halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/38—Separation; Purification; Stabilisation; Use of additives
- C07C17/389—Separation; Purification; Stabilisation; Use of additives by adsorption on solids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C21/00—Acyclic unsaturated compounds containing halogen atoms
- C07C21/02—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds
- C07C21/18—Acyclic unsaturated compounds containing halogen atoms containing carbon-to-carbon double bonds containing fluorine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US95719307P | 2007-08-22 | 2007-08-22 | |
| US957193P | 2007-08-22 | ||
| US196207 | 2008-08-21 | ||
| US12/196,207 US9035111B2 (en) | 2007-08-22 | 2008-08-21 | Method for producing fluorinated organic compounds |
| PCT/US2008/074033 WO2009026526A1 (en) | 2007-08-22 | 2008-08-22 | Method for producing fluorinated olefins |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2655871T3 true ES2655871T3 (es) | 2018-02-22 |
Family
ID=39926383
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES08798495.1T Active ES2655871T3 (es) | 2007-08-22 | 2008-08-22 | Método para producir olefinas fluoradas |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US9035111B2 (de) |
| EP (2) | EP2178814B1 (de) |
| JP (1) | JP5926488B2 (de) |
| KR (6) | KR20150117705A (de) |
| CN (2) | CN105753630A (de) |
| ES (1) | ES2655871T3 (de) |
| LT (1) | LT2178814T (de) |
| MX (1) | MX2010001605A (de) |
| PL (1) | PL2178814T3 (de) |
| TR (1) | TR201802546T4 (de) |
| WO (1) | WO2009026526A1 (de) |
Families Citing this family (41)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9024092B2 (en) * | 2006-01-03 | 2015-05-05 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US20230150900A1 (en) * | 2004-04-29 | 2023-05-18 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US8952208B2 (en) | 2006-01-03 | 2015-02-10 | Honeywell International Inc. | Method for prolonging a catalyst's life during hydrofluorination |
| US8664455B2 (en) | 2008-08-08 | 2014-03-04 | Honeywell International Inc. | Process to manufacture 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) |
| US9035111B2 (en) | 2007-08-22 | 2015-05-19 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| US9079818B2 (en) | 2007-10-15 | 2015-07-14 | Honeywell International Inc. | Process for synthesis of fluorinated olefins |
| BRPI0914033A2 (pt) * | 2008-10-13 | 2015-11-03 | Dow Global Technologies Inc | processo de uma etapa para a produção de de propenos clorados e fluorados e processo para preparar 2,3,3,3- tetrafluorprop-1 eno( 1,3,3,3- tetrafluorprop-1 eno (hfo-123ze) |
| BR112012007914A2 (pt) * | 2009-10-09 | 2019-09-24 | Dow Global Technologies Llc | reator isotérmico de tubos múltiplos, processo para produzir um propeno clorado ou fluorado e processo para preparar 2,3,3,3- tetrafluorprop-1-eno (hfo-1234yf) ou 1,3,3,3- tetrafluorprop-1-eno (hfo-1234ze) |
| KR20120093857A (ko) * | 2009-10-09 | 2012-08-23 | 다우 글로벌 테크놀로지스 엘엘씨 | 염화 및/또는 불화 프로펜의 제조 방법 |
| EP2485997B1 (de) | 2009-10-09 | 2015-09-09 | Dow Global Technologies LLC | Verfahren zur herstellung von chlorierten und/oder fluorierten probenen und höheren alkenen |
| EP2499110B1 (de) * | 2009-11-10 | 2020-02-26 | Daikin Industries, Ltd. | Verfahren zur reinigung von 2,3,3,3-tetrafluorpropen |
| CN102770400B (zh) | 2010-02-12 | 2015-09-30 | 大金工业株式会社 | 制备含氟烯烃化合物的方法 |
| HUE032122T2 (hu) | 2010-03-10 | 2017-08-28 | Arkema France | Eljárás fluorozásra folyadékfázisban |
| JP5899227B2 (ja) * | 2010-10-22 | 2016-04-06 | アルケマ フランス | ２，３，３，３−テトラフルオロプロペンの製造方法 |
| US8741828B2 (en) | 2011-02-23 | 2014-06-03 | Honeywell International Inc. | Azeotrope and azeotrope-like compositions useful for the production of haloolefins |
| CN102199071B (zh) * | 2011-04-08 | 2013-05-01 | 北京宇极科技发展有限公司 | 一种2,3,3,3-四氟丙烯的合成方法 |
| CN103562164B (zh) | 2011-05-31 | 2016-04-20 | 陶氏环球技术有限责任公司 | 生产氯化丙烯类的方法 |
| US9056808B2 (en) | 2011-05-31 | 2015-06-16 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
| WO2012170239A1 (en) | 2011-06-08 | 2012-12-13 | Dow Agrosciences, Llc | Process for the production of chlorinated and/or fluorinated propenes |
| US9233896B2 (en) | 2011-08-07 | 2016-01-12 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
| CN103717559A (zh) | 2011-08-07 | 2014-04-09 | 陶氏环球技术有限责任公司 | 生产氯化的丙烯的方法 |
| EP2782889B1 (de) | 2011-11-21 | 2016-12-21 | Blue Cube IP LLC | Verfahren zur herstellung von chlorierten alkanen |
| WO2013082404A1 (en) | 2011-12-02 | 2013-06-06 | Dow Global Technologies, Llc | Process for the production of chlorinated alkanes |
| IN2014CN04029A (de) | 2011-12-02 | 2015-10-23 | Dow Global Technologies Llc | |
| JP6170068B2 (ja) | 2011-12-13 | 2017-07-26 | ブルー キューブ アイピー エルエルシー | 塩素化プロパン及びプロペンの製造方法 |
| US9169177B2 (en) | 2011-12-22 | 2015-10-27 | Blue Cube Ip Llc | Process for the production of tetrachloromethane |
| BR112014015123A2 (pt) | 2011-12-23 | 2017-06-13 | Dow Global Technologies Llc | processo para a produção de um ou mais alcenos ou compostos aromáticos |
| EP2812298A4 (de) | 2012-02-10 | 2015-09-16 | Haiyou Wang | Verbessertes herstellungsverfahren für 2,3,3,3-tetrafluorpropen |
| WO2014046970A1 (en) | 2012-09-20 | 2014-03-27 | Dow Global Technologies, Llc | Process for the production of chlorinated propenes |
| CN104755448A (zh) | 2012-09-20 | 2015-07-01 | 陶氏环球技术有限公司 | 用于制造氯化丙烯的方法 |
| US9795941B2 (en) | 2012-09-30 | 2017-10-24 | Blue Cube Ip Llc | Weir quench and processes incorporating the same |
| EP2911773B1 (de) | 2012-10-26 | 2017-10-04 | Blue Cube IP LLC | Mischer sowie reaktor und verfahren damit |
| US9512053B2 (en) | 2012-12-18 | 2016-12-06 | Blue Cube Ip Llc | Process for the production of chlorinated propenes |
| JP6251286B2 (ja) | 2012-12-19 | 2017-12-20 | ブルー キューブ アイピー エルエルシー | 塩素化プロペン生成のための方法 |
| EP2961722A2 (de) | 2013-02-27 | 2016-01-06 | Blue Cube IP LLC | Verfahren zur herstellung von chlorierten propenen |
| US9403741B2 (en) | 2013-03-09 | 2016-08-02 | Blue Cube Ip Llc | Process for the production of chlorinated alkanes |
| CN105026350A (zh) * | 2013-03-13 | 2015-11-04 | 霍尼韦尔国际公司 | 分级氟化方法和反应器系统 |
| WO2014158663A1 (en) | 2013-03-13 | 2014-10-02 | Arkema Inc. | Methods for purifying and stabilizing hydrofluoroolefins and hydrochlorofluoroolefins |
| GB201410174D0 (en) * | 2014-06-09 | 2014-07-23 | Mexichem Amanco Holding Sa | Process |
| GB2559056B (en) | 2015-07-17 | 2019-09-11 | Mexichem Fluor Sa De Cv | Process for preparing 245cb and 1234yf from 243db |
| GB2540427B (en) * | 2015-07-17 | 2017-07-19 | Mexichem Fluor Sa De Cv | Process for the preparation of 2,3,3,3-tetrafluoropropene (1234yf) |
Family Cites Families (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2637747A (en) | 1948-01-23 | 1953-05-05 | Purdue Research Foundation | Fluorination |
| US2724004A (en) | 1952-04-08 | 1955-11-15 | Goodrich Co B F | Preparation of 1, 1-difluoro-1, 2, 2-trichloroethane |
| US2931840A (en) * | 1958-11-25 | 1960-04-05 | Du Pont | Process for preparing 2, 3, 3, 3-tetrafluoropropene |
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| US8084653B2 (en) * | 2004-04-29 | 2011-12-27 | Honeywell International, Inc. | Method for producing fluorinated organic compounds |
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| US7189884B2 (en) * | 2004-04-29 | 2007-03-13 | Honeywell International | Processes for synthesis of tetrafluoropropene |
| US8067649B2 (en) * | 2004-04-29 | 2011-11-29 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
| WO2007019355A1 (en) | 2005-08-05 | 2007-02-15 | E. I. Du Pont De Nemours And Company | Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 2,3,3,3-tetrafluoropropene |
| WO2007019358A2 (en) | 2005-08-05 | 2007-02-15 | E. I. Du Pont De Nemours And Company | Process for the preparation of 1,3,3,3-tetrafluoropropene and/or 1,1,3,3,3-pentafluoropropene |
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| PT3336073T (pt) | 2006-01-03 | 2022-12-21 | Honeywell Int Inc | Método para produzir compostos orgânicos fluorados |
| US8071825B2 (en) * | 2006-01-03 | 2011-12-06 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
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| MX337217B (es) * | 2006-10-03 | 2016-02-18 | Mexichem Amanco Holding Sa | Procedimiento de dehidrogenacion-halogenacion para la produccion de (hidro)fluoroalquenos de c3-c6. |
| GB0625214D0 (en) * | 2006-12-19 | 2007-01-24 | Ineos Fluor Holdings Ltd | Process |
| US9035111B2 (en) | 2007-08-22 | 2015-05-19 | Honeywell International Inc. | Method for producing fluorinated organic compounds |
-
2008
- 2008-08-21 US US12/196,207 patent/US9035111B2/en active Active
- 2008-08-22 WO PCT/US2008/074033 patent/WO2009026526A1/en not_active Ceased
- 2008-08-22 PL PL08798495T patent/PL2178814T3/pl unknown
- 2008-08-22 CN CN201610111875.8A patent/CN105753630A/zh active Pending
- 2008-08-22 CN CN200880113487A patent/CN101835729A/zh active Pending
- 2008-08-22 KR KR1020157025789A patent/KR20150117705A/ko not_active Ceased
- 2008-08-22 EP EP08798495.1A patent/EP2178814B1/de not_active Revoked
- 2008-08-22 KR KR1020207007713A patent/KR20200032255A/ko not_active Ceased
- 2008-08-22 ES ES08798495.1T patent/ES2655871T3/es active Active
- 2008-08-22 KR KR1020197016487A patent/KR20190068646A/ko not_active Ceased
- 2008-08-22 KR KR1020107003840A patent/KR20100043084A/ko not_active Ceased
- 2008-08-22 KR KR1020187031748A patent/KR20180122046A/ko not_active Ceased
- 2008-08-22 EP EP17201398.9A patent/EP3301083A1/de active Pending
- 2008-08-22 KR KR1020177014940A patent/KR20170064564A/ko not_active Ceased
- 2008-08-22 JP JP2010522069A patent/JP5926488B2/ja active Active
- 2008-08-22 MX MX2010001605A patent/MX2010001605A/es active IP Right Grant
- 2008-08-22 LT LTEP08798495.1T patent/LT2178814T/lt unknown
- 2008-08-22 TR TR2018/02546T patent/TR201802546T4/tr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| KR20170064564A (ko) | 2017-06-09 |
| TR201802546T4 (tr) | 2018-03-21 |
| EP2178814A1 (de) | 2010-04-28 |
| JP2010536881A (ja) | 2010-12-02 |
| WO2009026526A1 (en) | 2009-02-26 |
| KR20150117705A (ko) | 2015-10-20 |
| KR20190068646A (ko) | 2019-06-18 |
| EP3301083A1 (de) | 2018-04-04 |
| JP5926488B2 (ja) | 2016-05-25 |
| PL2178814T3 (pl) | 2018-06-29 |
| EP2178814B1 (de) | 2017-11-29 |
| LT2178814T (lt) | 2018-03-12 |
| KR20100043084A (ko) | 2010-04-27 |
| US20090203945A1 (en) | 2009-08-13 |
| KR20200032255A (ko) | 2020-03-25 |
| MX2010001605A (es) | 2010-03-15 |
| CN105753630A (zh) | 2016-07-13 |
| CN101835729A (zh) | 2010-09-15 |
| KR20180122046A (ko) | 2018-11-09 |
| US9035111B2 (en) | 2015-05-19 |
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